Gene: SEMA3D ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519374
rs1057519374
SEMA3D
A 0.700 CausalMutation CLINVAR Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere's disease. 27876815

2017